Phyllospongianes A-E (-), five new scalarane derivatives featuring an unprecedented 6/6/6/5 tetracyclic dinorscalarane scaffold, along with the known probable biogenetic precursor, 12-deacetylscalaradial (), were isolated from the marine sponge . The structures of the isolated compounds were determined by analysis of spectroscopic data and electronic circular dichroism experiments. Compounds - are the first 6/6/6/5 tetracyclic scalarane derivatives to be reported within the scalarane family. Compounds , , and exhibited antibacterial activity against , , , , , , and with MIC values ranging from 1 to 8 μg/mL. Furthermore, compound exhibited significant cytotoxic activity on MDA-MB-231, HepG2, C4-2-ENZ, MCF-7, H460, and HT-29 cancer cell lines with IC values in the range between 0.7 and 13.2 μM.
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http://dx.doi.org/10.1021/acs.jnatprod.3c00218 | DOI Listing |
J Nat Prod
July 2023
Research Center for Marine Drugs, State Key Laboratory of Oncogenes and Related Genes, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.
Phyllospongianes A-E (-), five new scalarane derivatives featuring an unprecedented 6/6/6/5 tetracyclic dinorscalarane scaffold, along with the known probable biogenetic precursor, 12-deacetylscalaradial (), were isolated from the marine sponge . The structures of the isolated compounds were determined by analysis of spectroscopic data and electronic circular dichroism experiments. Compounds - are the first 6/6/6/5 tetracyclic scalarane derivatives to be reported within the scalarane family.
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